ACRP Certified Professional : ACRP-CP

Pass ACRP-CP Exam Cram

Exam Code: ACRP-CP

Exam Name: ACRP Certified Professional Exam

Updated: Jul 28, 2026

Q & A: 127 Questions and Answers

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ACRP ACRP-CP Exam Syllabus Topics:

SectionObjectives
Topic 1: Quality Management- Risk management
  • 1. Quality assurance
  • 2. Corrective and preventive actions
- Audit and inspection readiness
  • 1. Compliance monitoring
  • 2. Inspection preparation
Topic 2: Professional Responsibilities- Leadership and professionalism
  • 1. Professional ethics
  • 2. Decision making
- Communication and collaboration
  • 1. Stakeholder communication
  • 2. Cross-functional teamwork
Topic 3: Clinical Trial Operations- Study start-up activities
  • 1. Protocol implementation
  • 2. Site preparation
- Study conduct
  • 1. Participant management
  • 2. Safety reporting
Topic 4: Data Management and Documentation- Data integrity
  • 1. Query resolution
  • 2. Data collection
- Clinical trial documentation
  • 1. Essential documents
  • 2. Source documentation
Topic 5: Ethical and Participant Safety Considerations- Human subject protection
  • 1. Participant rights
  • 2. Informed consent
- Regulatory compliance
  • 1. ICH GCP adherence
  • 2. IRB and ethics requirements

ACRP Certified Professional Sample Questions:

1. A Phase I drug trial has been completed and preparations are being made to proceed to a Phase II trial. Who is responsible for revising the IB with this updated information?

A) Sponsor
B) DSMB/IDMC
C) Investigator
D) Health authority


2. A serious unexpected ADR is one:

A) That results in the death of the subject.
B) Where the severity of the reaction is not consistent with IB.
C) Severity and nature of the reaction is consistent with protocol.
D) That does not need to be reported to the IRB/IEC.


3. A quality assurance audit of the EDC system SOP revealed a deficiency. Which of the following is the MOST likely reason?

A) The number of unique eCRF templates was not specified.
B) The frequency of data backup was not defined.
C) The list of comparable technology solutions was not included.
D) The number of users with access was not defined.


4. Access to study documentation for auditors and inspectors during an audit or inspection at a clinical trial site is the responsibility of the:

A) CRC
B) Sponsor
C) CRA
D) PI


5. All site financial matters pertaining to a trial are listed in what document?

A) Financial disclosure
B) Signed contract
C) Informed consent form
D) Protocol


Solutions:

Question # 1
Answer: A
Question # 2
Answer: B
Question # 3
Answer: B
Question # 4
Answer: D
Question # 5
Answer: B

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